Clinical Trial Manager

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Lead the planning, execution, and oversight of clinical trial activities, ensuring delivery against timelines, budgets, and key study milestones. • Partner with cross-functional teams to develop and implement study-specific operational plans, processes, and procedures. • Build and maintain strong relationships with investigators, study sites, vendors, and key stakeholders to support successful study outcomes. • Monitor study progress, proactively identify risks, and implement mitigation strategies to ensure continued operational excellence. • Ensure studies are conducted in accordance with ICH-GCP guidelines, protocol requirements, and all applicable local and international regulatory standards. • Oversee vendor performance and contribute to vendor selection, management, and governance activities where appropriate. • Drive issue resolution and support critical decision-making related to study conduct, quality, and operational delivery. • Act as a key point of contact for internal and external stakeholders, providing regular updates on study progress, risks, and achievements.

🎯 Requirements

• A degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related scientific discipline, or an equivalent combination of education and relevant experience. • Demonstrated experience leading the operational delivery of clinical trials and driving study outcomes against key performance indicators. • Strong understanding of clinical trial regulations, ICH-GCP requirements, and industry best practices. • Experience working within a commercial pharmaceutical, biotechnology, or CRO environment. • Prior clinical monitoring experience is advantageous. • Significant experience managing Oncology clinical trials, ideally within late-phase development programmes. • Excellent communication, organisational, and problem-solving skills, with the ability to influence and collaborate across diverse stakeholder groups.

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways